A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863733



Internal ID22638668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27666910..27670709hg38UCSC Ensembl
chr12:27819843..27823642hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465737
Samples
Known GenesPPFIBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863733
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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